7Li and 31P magic angle spinning nuclear magnetic resonance of LiFePO4-type materials

被引:71
作者
Tucker, MC [1 ]
Doeff, MM
Richardson, TJ
Fiñones, R
Reimer, JA
Cairns, EJ
机构
[1] Univ Calif Berkeley, Energy & Environm Technol Div, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Ernest Orlando Lawrence Berkeley Natl Lab, Div Sci Mat, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
关键词
D O I
10.1149/1.1464505
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
LiFePO4 and LiMnPO4 have been characterized using Li-7 and P-31 magic angle spinning (MAS) nuclear magnetic resonance spectroscopy. LiFePO4 was synthesized by a hydrothermal route and LiMnPO4 was synthesized at high temperature in an inert atmosphere. Both compositions give rise to single isotropic Li-7 resonances. The MAS isotropic peak linewidth for LiFePO4 is considerably larger than that for LiMnPO4, suggesting the presence of local disorder in the Li coordination sphere for LiFePO4. In both samples, the isotropic peak is accompanied by a large, asymmetric spinning sideband manifold, arising from bulk magnetic susceptibility broadening and the paramagnetic interaction between the lithium nucleus and transition metal unpaired electrons. (C) 2002 The Electrochemical Society.
引用
收藏
页码:A95 / A98
页数:4
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